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Kind
Tree Productions, Inc.
Autism
Newsletter
2005 - 2006
REACHING
OUT -
REACHING IN |
|
"Autism
Rocks" T-shirts!!

Note Cards by
people with autism |
Archives 2005 - 2006 / Archives
1998 - 2004
March, 2006 / June
2006 / October 2006
March 2005 / July 2005 /
September 2005
October,
2006 - In This Issue: sponsored by Autism
Speaks
Calling
All Americans / Mary-Minn's Stim
Page / Holiday Shopping with KindTree
What is Risperdal? / Autism
Speaks / Voter Disenfranchisement
Society spreads autism awareness /AAPC
cancelled the Oct 13 Autism Conference
VSA Arts Call for Poets and Musicians / Retreat
2006 Reflections
2006 Volunteer and Donor Thank You List
Community
Calendar
Autism
Rocks 3rd Annual
Mask Making Party
Saturday, Oct 28, 2 - 5 PM,
Cozmic Pizza, Downtown
Center Stage Karaoke
Prizes, Toys, Raffle
Make your own
Mask
Wear your own Costume
Sing your own Song
$5/person - $15/family
Be Part of
the Autism Community |
|
| 'Calling
All Americans'
If you watch TV, you’ve noticed - it’s election
season again. “I’m for the schools’, “It’s
the kids that matter”, “Honesty, trust, in-tegrity.”
I’m sure you’ve seen them. So many advertisements
spouting slogans or trying to make the other guy look bad.
It’s hard to have respect for that kind of thing.
Yet, next year’s legislative session is very important
to the autism community. Local school funding depends on
the State recognizing and prioritizing our needs - and having
the cash. Issues with the new mental health parity rules
will come up. The national level will see autism research
get funding attention - maybe.
How can I help? I can send you to Debbie Koch (debbiek@mcmc.net)
who is starting up an autism political action group in Ore-gon,
and to the Oregon Developmental Disabilities Coalition Oregon
voter guide here: http://www.oregonddcoalition.org/?q=node/175
And I can tell this one, small story. The rest is up to
you, fellow American.
A few weeks ago the organization Autism Speaks held their
first ever Eugene Autism Walk to raise money for their research
proj-ects. Organized by Teri Baker, a local parent, it was
a fine success, bringing together enthusiastic members of
our autism community. Teri tapped state senate candidate
Jim Torrey as the honorary chairman. Mr. Torrey arrived
a few minutes before the walking began and approached me
(I must have looked like I knew something - maybe it was
my Au-tism Rocks T-shirt). He asked me about autism. I appreciated
his interest even while I was disappointed that he seemed
to know so lit-tle. During his short talk, he repeated much
of what I had told him. He was leaving the impression autism
had been an important interest of his. He asked, “Where
is the media?” They came after he was finished.
I believe we need office holders who are sincere in their
belief that we can do good things if we are honest and trusting
with each other. I believe well trained, decently paid educators
require real money to stay in the difficult field of Special
Ed, and that real money doesn’t come from thin air.
I believe we’re all in this together. Are you ready
to really help us out, Jim?
|
|
Teddy's
Hobby Horse
Josh Breedlove
One of KindTree's
Holiday Cards Sets
We have a great issue today, with a fine story from Mary-Minn,
pictures from our largest-ever Autism Camp/Retreat, our
annual Volunteer and Donor thank you list, our 2006 Holiday
Card offerings, other news and events, and some great information
from Autism Speaks, who, through a donation of over $700,
are the sponsors of this issue of Reaching Out - Reaching
In. THANK YOU! Enjoy...
Tim Mueller |
VISIT eSCRIP
and Help Us OUT!! / Or print the sign up form HERE
Mary-Minn's
Stim Page
(Here are personal stories
about autism. If you would like to see your musings on this
page, please email Mary-Minn at sirag@mindspring.com.)
Workin' For
a Livin'
1978 was a banner year for me in sheer
quantity of jobs held. That year, I blew through 12 jobs
“like they were Kleenex,” as my older brother
put it. I was living in Manhattan, studying life sculpture
during evenings at the Art Students’ League on West
57th Street, sharing an apartment on the Upper East Side
with my parasitic boyfriend and making ends meet catch-as-catch-can.
The pinnacle of my career that year was waiting tables at
the Veracruz Spanish and Mexican restaurant, down the street
from the U.N. It was a mighty soft gig for the maladroit
waitress that I was. I’d show up at a leisurely 10:30
a.m., when I and my counterpart, a chivalrous Mexican man,
would set to work scouring the bathrooms and setting up
our stations before getting to the paid work of waiting
tables. Our choice clientele of U.N. diplomats were pleasant,
interesting to talk to, easy to wait on, and generous with
their tips. |
|
"Health
and safety standards were quite beside the point at the
Chocolate Factory. Being germ phobic, I threw out the dropped
chocolate when nobody was looking. "
At the end of our shift, we employees would be treated to
a substantial and delicious Spanish and/or Mexican dinner,
com-plete with potent and flavorful margaritas. No matter
that I was paid a mingey $3 a day, for which I signed the
back of a check; no matter that I was forbidden to look
at the front of the check, which probably was written for
a significantly larger amount. Wages were merely a maraschino
cherry perched precariously atop the proverbial ice-cream
sundae, as I made as much in tips during those three hours
as I would have been paid as a full-time filing clerk in
the dingy recesses of Wall Street or a proofreader for an
uptight fashion magazine in midtown.
About three weeks into my employment, my fellow waiter mysteriously
failed to show up for work, but I managed to get my friend
hired in his stead. She was an elegant Iranian woman with
patrician manners, in stark contrast to scrawny, tweaky,
fash-ion-dork me. My boss was clearly impressed by her.
She refused to clean toilets; my boss reassured her that
I could take up her slack, no problem. I objected strenuously.
I was not above cleaning toilets, but it was the “principle”
of having to show up a half-hour early to do a junior co-worker’s
“dirty work.”
The following Monday, our entire kitchen staff had vanished
from the face of the kitchen. The I.N.S. had deported the
lot of them, as had probably befallen the waiter. That Monday
turned out to be the busiest day I had ever experienced
at that establishment. The line was 20 or so people long.
Food was a long time coming, as my boss was ill-equipped
to keep up with such a barrage of orders by himself. I reassured
my patient cus-tomers that there was a slight problem in
the kitchen, that I hadn’t forgotten their order.
As usual, they were patient and kind with me.
When the food was finally ready, my supervisor brought it
to them with a magnanimous flourish and yelled at me in
front of the whole dining room for being so slow on the
uptake. I shrieked back at him, again in full view and earshot
of the entire din-ing room, that the food had been delayed
because we were without a kitchen staff, and not due to
any slowness of mine. I added that he should consider hiring
people with legal visas next time, even if he had to pay
them minimum wage. I was fired the next day for insubordination.
It wasn’t the first or the last job from which I was
fired, for one reason or other. Back then, employment was
easy-come-easy-go. I canvassed door-to-door for work rather
than bothering with the voluminous classifieds and employment
agencies, with their nitpicking requirements for shorthand,
which I had never studied, and for fast and accurate typing,
which I wasn’t to master until the corrasable IBM
Selectric II erased my terror of typos and Liquid Paper.
Within a week, I was working retail at a small “chocolatier”
deceptively named “The Chocolate Factory” on
Canal Street, back then a sleazy no-zone between the Bowery
and Wall Street. The boss was a questionable fellow named
Alan Silver, whom I renamed “Alan Silverfish.”
We employees shared a delirious, delicious and well-deserved
contempt for the Silverfish, but I was the only one with
the “guts” to call him that to his face, as
though my vocal disapproval could reform him, thereby making
the world a friendlier and safer microcosm. Self-righteous
“honesty”, above all, was a guiding principle
for me back then.
The Silverfish pretended to be a chocolatier, rather than
the mere purveyor of low-grade chocolate he was. To prove
his nonexistent culinary expertise, he had placed a small
saucepan with some somewhat dusty melted Hersheys atop a
hot plate in a small closet at the back of the store. In
reality, the chocolate he sold was imported, from across
the Hudson River–Brooklyn, to be exact. We were instructed
to tear down the chocolate boxes so that nobody could see
their origin. Whenever we needed something that our Brooklyn
supplier didn’t carry, the Silverfish would send Claire,
the prettiest and calmest among us, to trade shows under
an independent guise, as none of the other chocolate suppliers
would have any financial dealings with Mr. Silver. Claire
must have been one smooth talker to get into those trade
shows without a wholesalers’ license.
I took great pride in my ability to estimate weight precisely
to the ounce. Seeing this, my boss ordered me to overweigh
by a quarter pound, so as to sell more chocolate than the
customer had ordered. Sure enough, most customers didn’t
notice the slightly larger quantity I had “misweighed,”
but it chafed at my autistic love of precision.
New York City was still recovering from a long garbage strike.
“No spitting” signs adorned the streets and
subway stations, and for good reason. When chocolate fell
on the floor, we were instructed to dust it off and put
it back in the case. Health and safety standards were quite
beside the point at the Chocolate Factory. Being germ phobic,
I threw out the dropped chocolate when nobody was looking.
The store had a basement and sub-basement out of an early
Stephen King novel, inhabited by tomcat-sized rats with
sharp incisors and eyes that flashed red when the lighting
was just dingy enough. Claire and I were charged with penetrating
these sub-terranean reaches to retrieve the second-hand
heart-shaped boxes festooned with battle-fatigued ribbons.
Those hastily assembled, ratty boxes were just another of
love’s cruelties.
Every so often, Mr. Silver exhibited great generosity by
sending me out to an excellent little Chinese deli to fetch
low-mein for his crew. Those evenings, my till would come
out $20 or so short, which was a prodigious shortfall, considering
that the average purchase was $3.
A few days after a hectic Valentines Day, I gave notice
to my boss. Shocked that I not only had shown up for work
that day but had given him notice, Silverfish gave me a
severance bonus, plus a bag of chocolates. The bonus added
up to the amounts he had deducted from my pay for “over
rings.” And so, it was my turn to be shocked.
Mary-Minn Sirag
Read more of Mary-Minn's
Stim Pages HERE
What
do You want for Christmas?
NEW T-SHIRT COLORS-
RED and ladies cap sleeve style in GREY
Sage Green and Black still available
Some in kids’ sizes
$15-$18 each plus shipping. See
here... |
|
|
|
| KindTree Logo and Art Imprint Items - More
here... |
|
|
|
|
|
|
|
And here are the other three Holiday Cards
a set of 12 for $22.
Order Here... |
Carl Kinney

This set includes 2 each of six Z-ville characters
and their holiday 'song'. |
Frank Flanders
 |
Dorothy Bucher

|
| FDA
Approves the First Drug to Treat Irritability Associated
with Autism, Risperdal
The U.S. Food and Drug Administration
(FDA) today approved Risperdal (risperidone) orally
disintegrating tablets, an adult antipsychotic drug,
for the symptomatic treatment of irritability in autistic
children and adolescents. The approval is the first
for the use of a drug to treat behaviors associated
with autism in children. These behaviors are included
under the general head-ing of irritability, and include
aggression, deliberate self-injury, and temper tantrums."This
approval should benefit many autistic children as
well as their parents and other care givers,"
said Steven Galson, M.D., director of FDA's Center
for Drug Evaluation and Research. "Our agency
strongly encourages the development of appropri-ate
pediatric labeling for adult drugs, and Risperdal
is a wel-come addition to the growing number of such
products that have been shown to have an appropriate
risk-benefit profile when tested in children."The
product's effectiveness in the symptomatic treatment
of irritability associated with pediatric autistic
disorders was established in two 8- week, placebo-controlled
trials in 156 patients aged 5 to 16 years, 90 percent
of whom were 5-12 years old. The results, which were
evaluated using two assessment scales, showed that
children on Risperdal achieved significantly improved
scores for certain behavioral symptoms of autism compared
to children on placebo. The most common side effects
of the use of Risperdal included drowsiness, constipation,
fatigue and weight gain.
Risperdal is marketed by Janssen, L.P. in Titusville,
NJ. |
|
Community
Calendar
October 24,
Bridgeway House - Boys Social Group II
Nathelle Comeau, M.S. from Willow Learning Center
will be heading a new boy’s social group. The
first meeting will be Thursday, October 24th at 4
p.m. For more information, please call 345-0805.
At Bridgeway
House: 1st and 3rd Tuesday nights - Parent
support group. 1st Saturdays, 11:30 am: Exploring
Aspergers Syndrome with Nan Lester. Many more BWH
gatherings at www.bridgewayhouse.org
October 28,
2 - 5PM, KindTree Mask
Making Party, Cozmic Pizza. Fun for All. More Info
here....
November
1 - ASO-LCC membership meeting: 6:30pm, Bridgeway
House.
November
15th - AAPC conference River Ranch Event
Center Eugene, OregonMedical Supports and Interventions
for Children and Youth with Autism Spectrum Disorder.
Featuring local author Kristi Sakai. www.asperger.net
to register.
|
| This issue of Reaching Out - Reaching
In is sponsored by Autism
Speaks
We truly appreciate their interest in
our local community, and thank them deeply for their
financial support of our Autism Retreat 2006 |
|
A Letter to KindTree
On behalf of Autism Speaks, Scott Ryan and I are grateful
for the opportunity to support local ASD organizations and
ASD activities, such as the Autism Camp/ Retreat hosted
by KindTree Productions this past August. There are few
joys that are equal to seeing a smile on the face of child
with autism. The day Scott and I visited the ASD summer
camp at Baker’s Boy Scout Camp was especially joyful,
as there were more smiling faces than I could count!
Thank you for welcoming Scott and I at your Saturday night
buffet. We were honored to be your guests. But most of all,
thank you for your support for Autism Speaks’ inaugural
“A Walk for Autism Research in Eugene” on Sunday,
September 10th. The combine Walks in Eugene and Portland
(held the day before) raised more than fifty thousand dollars
for autism re-search.
Of the fifty research projects funded this year through
Autism Speaks, two autism projects are right here in Oregon.
One is at Oregon Health Sciences University (OHSU), the
researcher is Dr. John Welsh, and the other project is in
our backyard at the University of Oregon, the autism researcher
is Dr. Philip Wash-bourne. For more information regarding
autism research, please log on at autismspeaks.org and click
on Science.
Autism Speaks and NAAR (National Alliance for Autism Re-search)
are actively recruiting the brightest and most talented
researchers for the sole purpose to find a cause and cure
for this life altering disorder. There are many autism research
projects being conducted all over the world, and Oregon
has taken a huge step toward contributing to finding this
cause and cure for all our children. Thank you.
Teri Baker
For Teens and
Adults
As your child enters his adolescent years, expect
him to find this time period challenging, if not downright
difficult. After all, even kids who aren't on the
spectrum are daunted by the formidable transition
between childhood and adulthood, and it's even trickier
for those who are autistic.
Autistic teens are befuddled by physical and hormonal
changes in their bodies, by developing social circles
and by increasing contact with the world at large.
They're also wrestling with complicated emotions.
Adolescence is when, according to the National Institute
of Mental Health, they “may become painfully
aware that they are different from their peers,”
a realization they may not be fully prepared to face.
As a result, they may appear to regress, acting out
and exhibiting behaviors, such as hitting or rocking,
they may have conquered long ago.
Riding an Emotional Rollercoaster
Your child may lean on you more as he navigates
the years ahead so prepare for the rollercoaster of
emotions on which he may soon embark. Let him know
that you're there to guide him through any situation
he may find uncomfortable. Ask the opinions of his
teachers, who will help him master new skills so he'll
be better equipped to interact with his peers and
take on bigger responsibilities.
Teen mentoring programs such as the one run by the
University of Washington Autism Center can teach him
or her how to be more comfortable in social situations
so he or she will know how to move in environments
that may not be as familiar as home or school. You
may also want to consider sending your child to a
summer program espe-cially designed for autistic teens,
such as the Talisman Camp or the Stone Mountain School,
both in North Carolina, where he can meet other teens
on the spectrum.
With ample support and encouragement, your child
stands a good chance of overcoming the initial pressures
and in time, he'll learn how to adjust to his shifting
landscape.
Stepping into Adulthood
Once your child is an adult, his options will depend
on how high functioning he is. When he has “aged
out” of public school, a vocational training
program may be the next best step.
Depending on his capabilities, he may excel at jobs
that require enormous amounts of concentration but
limited intense interaction with others, such as computer
programming or graphic design. Or, he may prefer to
do something more repetitive, such as filing. If he's
academically rigorous, college may be the answer.
(Temple Grandin, an autism activist who's on the spectrum
herself, is a renowned professor of animal science.)
In short, he or she is only truly limited by his
or her own abilities and interests, which holds true
whether one is autistic or not.
|
|
Our
Mission
At Autism Speaks, our goal is
to change the future for all who struggle with autism
spectrum disorders.We are dedicated to funding global
biomedical research into the causes, prevention, treatments,
and cure for autism; to raising public awareness about
autism and its effects on individuals, families, and
society; and to bringing hope to all who deal with
the hardships of this disorder. We are committed to
raising the funds necessary to support these goals.Autism
Speaks aims to bring the autism community together
as one strong voice to urge the government and private
sector to listen to our concerns and take action to
address this urgent global health crisis. It is our
firm belief that, working together, we will find the
missing pieces of the puzzle.
Voter
Disenfranchisement BillH.R. 4844 Passes House, Not
Brought Up by Senate
Right-wing members of the House continued their assault
on voting rights by passing H.R. 4844, “The
Federal Election Integrity Act.” This bill,
aimed at partisan advantage in future elections, would
place extremely onerous voter identification requirements
on voters, forcing them to obtain ID’s that
prove their citizenship. Disguised as a measure to
combat massive voter fraud that simply does not exist,
it would disenfranchise possibly hundreds of thousands
of primarily elderly, poor, minority, disabled and
student voters. We feared congressional leaders would
try to sneak this through the Senate by attaching
it to a must-pass appropriations bill for either Homeland
Security or Defense, but that did not happen.
PEOPLE
FOR THE AMERICAN WAY October 3, 2006
Society
spreads autism awareness September 21, 2006
The Help Autism Now Society is distributing materials
to Oregon doctors this week to help doctors and parents
more easily recognize and diagnose the disease.
Posters, illustrated books and other materials will
be sent to about 2,000 doctors throughout Oregon to
promote earlier detection of au-tism, a condition
that affects a child's ability to communicate and
so-cially interact.
There is no lab-based test to determine autism, so
observation remains the primary tool for its diagnosis,
said Linda Lee, the executive direc-tor of the society.
See the material: www.helpautismnow.com.
AAPC
cancelled the Oct 13 Autism Conference, so
sorry! The November 15th AAPC con-ference in Eugene
at the same location is still on, however. Anyone
who already registered for the Oct. 13th conference
will receive a full refund and a gift certificate
good toward the purchase of books, as well as a $25
dollar off coupon for the Novem-ber Conference:Medical
Supports and Inter-ventions for Children and Youth
with Autism Spectrum Disorder. See Community
Calendar |
The
Things I'm Forced to See By Gabby Green-Nickerson,
Age 14, California
Just
fifteen steps to the piano bench, I thought to myself as
I walked. I felt around to find where I was. I hit the bench
with a noticeable thump, and felt the heat rise up in my
cheeks. I sat down. My fingers danced over the ivory and
ebony keys, as I knew them to be, which I could picture
perfectly in my head. I hit a key, hoping I had found the
right one. Perfect. I smiled and, by memory, carried on
my solo.My solo. My solo.
(Excerpt from The Things I'm forced to See, 2005.)
VSA arts
International Young Soloists Award
Calling all rock stars & hipsters... virtuosos
& divas... jazz bands and blues brothers... MUSICIANS
OF ALL STYLES!!!
EligibilityAny individual musician (instrumental or
vocal) from the United States who has a disability,
age 25 and under, is eligible to apply. Any individual
musician (instrumental or vocal) from outside the
United States who has a disability, age 30 and under,
is eligible to apply. Individual musicians should
complete the Individual Musician Application Form.
Applications from musical ensembles (two to eight
members) will be accepted for the International Young
Soloists Award. This includes any type of ensemble
from a rock band to a chamber ensemble to a drum corps.
In order to be eligible, at least one member of the
ensem-ble must have a disability. All members of the
ensemble must fulfill the age requirements as stated
above. The ensemble should complete the Ensemble Application
Form.
All types of music will be accepted, including but
not limited to Rock/Alt Rock, Pop, Indie, Classical,
Country/Folk, Jazz, R&B/Blues, Hip Hop/Rap, Latin,
World, etc.
Deadlines:
December 1, 2006 for U.S. applicants
December 15, 2006 for applicants outside the U.S.
www.vsarts.org
for more information |
|
VSA
arts International Call For Flash Fiction, Poetry
and Spoken Word
The ultimate goal: your mind in words.
Flash fiction is an especially short story that
gets at the core—a microscope’s view of
the world.Writing poetry is an act of discovery, not
just words laid out in lines.
Spoken word is your lyrical voice, your inner thoughts,
and energy emerging through poetic performance.
The Theme - “A Moment in Time: Zooming In on
My Life”
Create a short story, poem, or spoken word performance
that zooms in on a specific moment in your life, as
a photographer zooms in on a subject to capture intricate
details. Choose an extraordinary OR an ordinary moment
from your life. Take a walk through your past, the
memories of your mind: watching a fluttering butterfly;
witnessing a car crash; smelling the pages of a new
book; riding your bike and getting lost; sipping your
mom’s hot chocolate in the winter. Relive an
experience where you felt adrenaline, elation, discomfort,
or contentment. What life experience has shaped you?
All poetic forms, fictional experiments, and spoken
word performances are welcome.
Deadline: December 8, 2006 |
Camp / Retreat
2006







|
|
"Jon and I are getting some good things growing
with a group of care givers in Eugene who actually
love excuses to have autistic get together's where
everyone can sing, do drumming, do art, freak out
and only get mellowness, love and acceptance from
everyone else. It's such a wonderful bunch of people.
Athena was at her VERY WORST at their last retreat.
I couldn't socialize, go to the talent show, the drumming
circle or all the other fun stuff that they were doing.
Athena was too crazy so we spent a lot of time walking
around or staying in our tent.
However, during all that mess, people would come
up to us with interest, sympathy for Athena and acceptance
and affirmation about what she's going through. They
treated her like a likable person and made us feel
a big sense of belonging even though I didn't have
much energy to give much back to them. They asked
how they could make things better. I couldn't think
of anything but suggested that they sing Edelweiss.
So they did and Athena's mood changed to amazement
and she started laughing and singing, too. Then she
stopped being so mean. She was still not wanting to
be nice enough to walk among the masses but I think
that, along with her miserable mood, she'd been thinking
that everyone there must hate her because she was
being so anti-social. She got through the rest of
the retreat with a more cooperative attitude.
One event that happened when Athena was at her worst
was when I was setting up the tent. A boy rushed over
and tried to climb into the flat tent as though it
were a sleeping bag. His two care givers tried to
stop him and apologize, but Athena suddenly was so
cheered up by some good old fashioned impulsive autism
and he liked her tent so it meant that much more to
her. I told them to let him have his fun. So they
got into the fun and took lots of pictures. Then he
got out of the tent and run away with the care givers
chasing after him.
They have been creating retreats, concerts and traveling
art shows centered around autism for ten years and
now they want to do more in more areas.
They are so loved but when it comes to writing grant
requests, they worry so much that they'll do it wrong
and feel funny about competingwith everyone else who
wants money so they ask people for money in funny
informal ways and get it because people love them
so much.
Steve Edelson says he doesn't know of any other place
in the world where they say their mission is to celebrate
autism."
Becky Beach
Mark Your Calendar:
Camp/Retreat 2007 August 24-26, 2007 See
you there...
|
2006 Volunteer and Donor
Thank You List
Sundance Natural Foods
29th Street Market of Choice
Capella Market
Fred Meyer
Bi-Mart
Costco
Jerry's Home Improvement
Monaco Coach
Eugene Freezer and Storage
Emerald Valley Kitchens
Toby's Tofu Palace
Surata Soy
Organically Grown
Co-op
Jay Frazier
Tony Diaz
Nancy Bright
Erika and Olise Johnson
the Buffalo Exchange
|
|
Bagel Sphere
the Bread Stop
ASO
Alpha Omega Computers
Michael Omogrosso
T.R. Kelley and Randy Hamme
Patricia Smith
Autism Speaks
The Boy Scouts of America
Art Kennedy
Bridgeway House
Hannah Schneider-Lynch
Sarah Berkley
George Mueller
Emily and Ken Ross
The Wentworth Foundation
David Fuchs
Robert and Julie Pasley
Mayor Kitty Piercy |
|
Aria Mikkola-Sears
Amy Smolek
Rhonda, Alex and Tyler Way
Paula Stuart
Mary King
Beckie Smolek
Gary Cornelius
Dyan Campbell
Tim Mueller
Nel Applegate
Michelle Jones, and Tyson
Melissa Linville
Jeff and Sarah Fields
Nan, Dave, Oliver and Max Lester
Carlos Berrera
Joy
Daniel Deming
Zach Lyons
Josh Fraim and Colleen
John Roberts
VSA Arts |
|
Mary-Minn Sirag
Jeanne-Marie Moore
Joel Litersky
Deborah Thiessen
Neil Lyda
Johanna Magner
Franklin Michael
Donald Burton
Caleb W
Molly Elliot
Thomas Finney
Kelani Larsen
Jerry Linville
Tracy Rogan
Claire Zane Jennifer Doolittle
Dustin and Dixie
Karen Howe
LaFollette Gallery
Slug Queen Slugnostra
Paul Orbell
Anna Morrison
Lane Arts Council |
|
back to top
June,
2006
Into the
Future / Mary-Minn's Stim Page
/ Computers?
ASO-LCC Report / Retreat
Sponsorship / When False Hope can be Fatal
New Research Findings /18
Year-old's Enlistment Released / Call for
Art Entries
Sparkplug Dance / Community
Calendar
VISIT eSCRIP
and Help Us OUT!! / Or print the sign up form HERE
| 'Into
the Future'
This last winter the Oregon Department of Education informed
us that 1 in 98 Oregon students are on the Autism Spectrum.
Larry Sullivan of 4J school district tells us there are
260 students in his jurisdiction with current IEP’s
for autism. Each and every one of these kids needs support
now and most likely will continue to need them for the rest
of their lives.
Here in Lane County we are responding. In addition to strong
services from Autism Training and Support, Direction Service,
Lane Developmental Disabilities Office, the ARC of Lane
County, Eugene and Springfield’s schools systems,
and many private providers and consultants, we have non-profits
like Bridgeway House, the Aspergers Advocacy Coalition,
the ASO-Lane County Chapter and, new to our area, Autism
Speaks.
Each of these entities work in their own way to improve
the lives of people with autism, both now and for the future.
I urge you all to search them out, work with them, be an
active participant in our Autism Community.
Check our Community Calendar,
designed to help you find events that will enhance your
lives. KindTree’s website lists many local and national
links to other organizations that can inspire and inform.
With individual help from Direction Service, clinics and
support groups at Bridgeway House, seminars and trainings
from many different sources, recreation from KindTree and
the City of Eugene, respite help from the ARC, there are
so many ways to get help. Reach Out - someone will take
your hand.
|
|
Carl
Kinney - Chia Bush
See this and more at
"Art & the Vineyard"
Coming up at KindTree is our annual participation
in the Art
& the Vineyard festival, July 1-4. Come,
volunteer, buy art, support our autistic artists. Their
work is truly marvelous. August will bring our 10th
Autism Retreat. This event is so wonderful
I can hardly describe it. Families can be safe there, we
can all be ourselves there, “ Through the power of
self-advocacy in an atmosphere of acceptance and respect,
autistic and neuro-normal people alike can work toward self-
realization.” Sign up now before we fill up.
The local ASO-LCC chapter has initiated a new resource
on their website. You can search a growing database of local
resources, or add your own. There is no fee and directions
are clear. Stop by and visit at www.asolanecounty.org.
KindTree will also be represented at the Oregon Country
Fair in the Community Village. Working to grow tolerance
and understanding is a Village goal. That is definitely
a need for people with autism! See you there?
Tim Mueller |
Mary-Minn's
Stim Page
(Here are personal stories
about autism. If you would like to see your musings on this
page, please email Mary-Minn at sirag@mindspring.com.)
The anatomy
of a freakout
The first day after being ill is wonderful,
indeed. My senses are alert without being too sharp. My
brain can follow a logical pattern again. The temperature
outside not only is perfect, but feels perfect. Colors are
bright, and spring smells sweet again. I am well rested,
after 12 or so hours of sleep, and I could eat a house if
only a realtor would give me one to chaw on. My body is
clear of aches and pains.
My illness was a four-month flood of
high anxiety, depression and freakouts that crested just
last night with a skin-crawling darkness of the soul. It
started out insidiously as my customary winter depression.
|
|
"I
lost my ability to anticipate, recognize and ward off my
Confusion Triggers. "
My brain receptors had become immune to the antidepressant
I was taking, rendering it useless. I felt too delicate
to embark on yet another series of biochemical experiments
before hitting on another antidepressant that would hold
me until the next crash. Putting this off was my first big
mistake.
A friend of mine had successfully diminished a recent
trauma of her own with a five-session course of EMDR rapid-eye
movement cognitive therapy treatments, which heartened me.
I determined that I too could weaken my own freakout triggers
with a course of EMDR, since my triggers are specific: losing
things, getting lost, and not knowing what I am supposed
to do in any given moment. I had even figured out the specific
experiences leading up to my triggers. Thinking that five
sessions of EMDR would fix me was my second mistake.
In a metaphoric and less than scientifically rigorous
nutshell, the rapid eye movement, by stimulating both sides
of the brain almost simultaneously, rearranges trauma-induced
neural pathways that are activated by stimuli the patient
associates with the trauma. The goal is to scramble these
pathways sufficiently to disentangle the multitude of triggers
from the initial trauma. Later on in the process, reintegration
supposedly occurs after the brain has formed new pathways
that are squeaky-clean of the trauma and its ramifying surrogates.
The therapist provides the patient with a safe venue to
revisit these traumas as the patient’s eyes track
the therapist’s rapid back-and-forth hand movements.
After helping me to come up with comforting images to keep
in mind, my therapist told me to relax and follow my thoughts.
My first serious obstacle was that relaxation is a state
of being that is every bit as elusive to me as spiritual
enlightenment. My second obstacle was my extreme defensiveness
about opening my being to my traumas. Though I can ruminate
about them endlessly, voluntarily re-experiencing them in
a therapeutic context is a whole other matter. My third
obstacle was my innate suspicion of professionals, even
when I’m giving it my college best to be open-minded.
During the sessions, however hard I tried to revisit these
traumas of mine, my attention settled instead on comforting
stimuli–the reassuring tock of a mechanical clock,
the bells at St. Mary’s Episcopal Church that reminded
me of church bells in the village of my childhood, the warming
click of the baseboard heater, even a bus changing gears,
so reminiscent of cross-country Greyhound bus trips I took
during college. My therapist was astonished at how many
mechanical sounds I took refuge in. She clearly wasn’t
the John Cage fan that I am. Meanwhile, the trauma I was
trying so hard to reframe evaded my conscious grasp.
Alas, the therapy was worse for me than merely ineffectual.
As promised, my brain felt scrambled for a few weeks, which
was initially reassuring, as something seemed to be happening.
The awful part, though, was that it never unscrambled completely
to reintegrate its moorings, so my triggers became more
random and unpredictable than before. Perhaps the requisite
five expensive treatments were insufficient for my slow
processing of information; however, by then, I was done
with throwing good money–and time–after bad.
My mental health cascaded from there. My anxiety worsened
from mere agitation and nervousness to a pervasive sense
of im-pending doom and wrenched anguish. Daily, I awoke
in a cold sweat of panic and foreboding, dreading the day’s
unfolding. Premoni-tions of death loomed as I got behind
the wheel, and my mind perseverated on near-accidents. My
skin crawled as though trafficked by tiny vermin. My brain
felt ready to pop out of its skull. My innards clenched.
Things I had said reverberated back at me days later in
a hollow mockery of my voice. My heart raced as though my
veins were going to explode. I felt windswept from the inside.
I developed a gripping and galloping-stampede social phobia.
During the last week of my crisis, my anxiety culminated
in a low-grade fever that kept me unpleasantly hot, though
the ambient temperature was pleasantly cool. Toward the
very end of my long episode, I craved solitude but couldn’t
stand to be alone.
I lost the ability to keep things properly organized for
myself, which fed one of my two worst freakout triggers:
losing things. I couldn’t remember where I had–or
even should–put things. My visual processing and sense
of direction deteriorated, as did my problem-solving and
troubleshooting ability. For instance, I often neglected
to check the phone book and my various street maps before
venturing out into even slightly uncharted reaches, thinking
that “everything is going to be alright.” I
forgot to eat frequently enough, rendering me woozy, irrational
and irascible. Though I continued to print out my checklists
for leaving the house in the morning, I glossed over important
checkpoints and neglected to close important loops I had
opened, such as strapping my keys to my right-hand pocket
in order to keep myself safely attached to them.
During this four-month period, my freakouts increased
in frequency and intensity as I lost my ability to anticipate,
recognize and ward off my confusion triggers. Each freakout
left me raw and vulnerable to even worse subsequent ones.
They evolved from fits of obscene ranting and high-decibel
shrieking at my frozen-up computer; to stapling my wrist,
cross-hatching one arm with a serrated knife and bruising
the other with the clenched fist of the first hand; to a
stomping and shrieking rage of frustration and confusion-panic
at a dear friend and her family due to an unreasoned assumption
I had made in a state of hypoglycemic exhaustion.
My friend and her family accepted my abject apology. I
then dissected and analyzed my recent hell with her, other
friends and family. In place, yet again, are my protocols
of prevention: When my brain is slower than the world around
it, I am to request a smokeless break to sort and map things
out in my mind, to look up the address in the phone book
and the exact coordinates on a map. Whenever I leave the
house, I am to pack plenty of nourishing protein to fuel
my brain. Whenever I feel that hazard bubble ascending from
my gut to my brain, I am to stop and figure out what my
spider sense is trying to tell me.
As the egg man at the Marin County farmers’ market
told my sister, “Don’t be too hard on yourself.”
Mary-Minn Sirag
WANTED:
people who need computers!
KindTree’s Computer Exchange
program has grown. People and agencies all over the state
are sending people our way in search of computers. We have
some newer ones from Lane County. Call 521 7208 or computers@kindtree.org.
We need you. Want to volunteer to fix 'em up?
ASO-LCC
minutes excerpt, May 23, 2006
4-J Report.
Larry Sullivan:
There are presently 260 students on the spectrum with
current IEP’s in place. Larry’s district
has about 30 teachers so far who have taken a 4-J
professional development course to help them provide
appropriate services to students on the autism spectrum,
with more training to come in the fall, including
planned guest speakers. There is a focus to develop
“autism friendly buildings” within 4-j
that concentrate staff with special training to build
an understanding and productive environment. Cal Young
school is the focus at this time, with staff developing
a virtual case management style model.
Larry also spoke of a recent court decision that
prevents the district from implementing an after school
program for kids on the spectrum. The plan was an
after school “bridge to home” that could
function as a winding down place. The $30,000 funding
in place for this program fell away when a lawsuit
successfully argued that the district created the
levy that funded the program (and others) illegally.
Read more at www.asolanecounty.org
|
David
Olson
at Art & the Vineyard

Nick Gerlach
at Art & the Vineyard
|
Autism's
parent trap: When false hope can be fatal
By Cammie McGovern from The New York Times TUESDAY, JUNE
6, 2006
In recent weeks, three stories have hit the news with
grimly similar plot lines: parents accused of killing their
autistic children.
On April 12, in Hull, England, Alison Davies and her son,
Ryan, 12, fell to their deaths from a bridge over the River
Humber, in an apparent murder-suicide. (A note was found
in the Davies's kitchen.) On May 14, in Albany, Oregon,
Christopher DeGroot, 19, was trapped inside a burning apartment.
He died in a Portland hospital five days later, and his
parents are charged with murder, accused of locking their
son in the apartment alone. And on the same day, in Morton,
Illinois, Dr. Karen McCarron admitted to the police that
she had, the day before, suffocated her daughter, Katherine,
3, with a plastic garbage bag.
Any parent of a child with autism remembers, as I do,
reading every book, pursuing every lead and never taking
a night off - because autism feels like a war you rearm
yourself nightly to wage. Comments suggested the parents
may have been trying too hard. Perhaps they were frustrated
that their efforts did not lead to greater improvement in
their children. That would not be surprising, because dramatic
improvement is what too many parents are led to expect
Having an autistic child is estimated to cost a family
$10,000 to $50,000 a year for medical treatment, therapy
and education. With 50 new diagnoses of autism in the United
States every day (1 in 98 kids in Oregon’s schools),
support services are already too stretched to meet the need.
But as much as I'd like to fault government policy, I
suspect it is not entirely to blame. There's another issue
that hits closer to home and is harder for most parents
of autistic children to be candid about.
When your child's disorder is initially diagnosed, you
read the early bibles of hope: "Let Me Hear Your Voice,"
"Son-Rise" and other chronicles of total recovery
from autism. Hope comes from a variety of treatments, but
the message is the same: If you commit all your time, your
money, your family's life, recovery is possible. And who
wouldn't do almost anything - mortgage a home, abandon a
career or move to be closer to doctors or schools - to enable
an autistic child to lead a normal life? Now, as the mother
of a 10-year-old, I will say what no parents who have just
discovered their child is autistic want to hear, but should,
at least from one person: I've never met a recovered child
outside the pages of those old books. Not that it doesn't
happen; I'm sure it does. But it's extraordinarily rare
and it doesn't happen the way we once were led to believe.
Every parent of a child on the autism spectrum knows this
feeling: I've done everything possible; why isn't he better?
The answer is simple: Because this is the way autism works.
There are roadblocks in the brain, mysterious and unmovable.
In mythologizing recovery, I fear we've set an impossibly
high bar that's left the parents of a half-million autistic
children feeling like failures.
I don't mean to sound pessimistic about the prospects
for autistic children. On the contrary, I see greater optimism
in delivering a more realistic message: Children are not
cured, but they do get better.
And better can be remarkable. At 10, my son is a far cry
from the toddler who melted down when the sand was the wrong
texture for drizzling. These days he embraces adventure,
rides his bike, and repeats any story he tells five or six
times. I remember thinking maybe we'd laugh someday at the
lengths we went to when we were teaching him language -
the flashcards, the drills, the repetitions.
Now he's 10 and talking at last in his own quirky ways,
and we don't laugh about the drills (though we laugh about
plenty of other things). Language is a victory. So is connection
and purposeful play. So are the simpler things: a full night's
sleep, a tantrum-free day.
Parents working toward these goals will one day be surprised
and delighted by their children's funny new obsessions,
odd fixations and tentative but extraordinary connections
with other children.
Being more realistic from the start might make it possible
to enjoy the journey and to see it for what it is: helping
a child who will always function differently to communicate
better and feel less frustrated.
To aim for full recovery - for the person your child might
have been without autism - is to enter a dangerous emotional
landscape. For three children, the disconnect between parental
determination and limited progress may have been lethal.
Cammie McGovern is the author of "Eye Contact,"
a novel.
New
findings help pinpoint autism’s genetic roots
www.inovations
report 05.05.2006
By deleting a gene in certain parts of the brain, researchers
at UT Southwestern Medical Center have created mice that
show deficits in social interaction that are reminiscent
of humans with autism spectrum disorders. The investigators
also found physical abnormalities in the brains that mimic
some cases of autism, showing that the research animals
can be useful in studying the mysterious condition. The
finding — to be published in the May 4 issue of the
journal Neuron — confirms recent indications that
a mutation in this partic-ular gene could cause at least
some forms of autism, said Dr. Luis F. Parada, director
of the Center for Developmental Biology and the study’s
senior author. Dr. Parada also directs the Kent Waldrep
Center for Basic Research on Nerve Growth and Regeneration.
"The exciting thing about this mouse is it helps us
to zero in on at least one anatomic location of abnormality,
because we targeted the gene to very circumscribed regions
of the brain," he said. "In dis-eases where virtually
nothing is known, any inroad that gets into at least the
right cell or the right biochemical pathway is very important."
Read more at:
http://www.innovations-report.com/html/reports/life_sciences/report-58724.html
This research funded in part by NAAR - Autism Speaks
Army
releases 18-year-old with autism from enlistment contract
By SARAH SKIDMORE, The Associated Press, May 10, 2006
PORTLAND — An 18-year-old Portland
man with autism, whose recruitment renewed questions about
Army practices, was released Tuesday from his enlistment
contract.
Jared Guinther signed up for one of the Army’s most
dangerous jobs, cavalry scout, after being heavily recruited.
He passed medical and other examinations. He was scheduled
to leave for basic training in August.
The Army announced Tuesday that it decided he didn’t
meet enrollment criteria, two days after The Oregonian newspaper
reported his parents’ objections.
Gaylan Johnson, spokesman for the United States Military
Entrance Processing Command, said Guinther’s disability
was not disclosed in the medical exam and information regarding
his condition was not available to the command until after
the enrollment process was complete. The command oversees
medical exams for the Army.
Guinther’s mother told The Oregonian she informed
recruiters about her son’s disability by telephone
as Jared was being tested, but that he was accepted for
enlistment anyway.
An investigation is under way into whether recruiters improperly
concealed Guinther’s condition.
Guinther started talking about joining the military after
a recruiter stopped him and offered him a $4,000 signing
bonus and $67,000 for college, his parents say. His parents
said he didn’t know there was a war in Iraq until
last fall, shortly after he spoke with a recruiter, and
asked them about it.
The Army has been under intense pressure to recruit, and
the number of recruiting abuses hit record levels in recent
years.
In response to the Guinther case, Democratic Rep. Earl
Blumenauer of Oregon called on Secretary of Defense Donald
Rumsfeld to con-duct a broad investigation into military
recruitment practices and abuses.
In Guinther’s case, the Army had heavily recruited
him even though his disability should have disqualified
him from enlisting.
When Guinther’s parents found out he had enlisted,
they contacted the Portland U.S. Army Recruiting Station
where he signed up. His parents say the Army did not initially
respond to their concerns.
With the Guinthers’ permission, The Oregonian faxed
Guinther’s medical records to the U.S. Army Recruiting
Battalion commander, who ordered an investigation.
On Tuesday, the Army said it could not discuss the case
further because the investigation is under way.
Gary Stauffer, spokesman for the Portland Army Recruiting
Battalion, said the Army anticipates concluding the investigation
this week.
call
for entries - destination anywhere
A National Juried Exhibit for Young Artists with
Disabilities, Ages 16 – 25.
Deadline: Friday, July 14, 2006, midnight (MST)
Grand Prize: $20,000
First Award: $10,000
Second Award: $6,000
12 Awards of Excellence: $2,000
Sponsored by VSA arts with generous assistance from Volkswagen
of America, Inc.
More info: Here...
KindTree would like to help. Any qualifying
artist can contact KindTree and we will help you get your
art entered.
Call 541 521 7208 or e-mail entry@kindtree.org
Yes We Can.
Sparkplug
Dance and Adaptive Recreation Summer Camps
Sparkplug Dance, in cooperation with the City of Eugene's
Adaptive Recreation Department, received an award from The
Lane County Cultural Coalition from funds provided by the
Oregon Cultural Trust. The award will provide early childhood
professionals, teachers, and teaching artists from Lane
County with a fall workshop in inclusion-based arts education
for preschool and elementary students.
This summer Sparkplug Dance and Adaptive Recreation is
offering two summer camps designed for youth of all abilities.
In the Multicultural Camp (7/17-7/21),
we'll explore the dance, sto-ries, and art of Australia,
Africa and the Pacific Northwest Coast! And in our Dance
and Art Camp (7/24-7/28), we'll make plaster masks,
murals, and collages, and explore nature in art, relating
each day's activities to dance. For more information, contact
Hilyard Center at 682-5311.
COMMUNITY
CALENDAR
June 17, Employment
Workshop: 9:00 am— ”Beating the
Odds”, presented by Cynthia Owens
10:30 am— ”Changing lives through employment!
All can work, how do you make it a reality?” Presenter:
Paul See
Gateway Elks Club. kathyh@arroautism.org Or call: 503-284-0350
Monday-Friday
June 26-30, Autreat by ANI Philadelphia, Pennsylvania.
www.ani.autistics.org
July 1-4 all
day Art & the Vineyard Autism
Rocks Traveling Art Show.
At Autism Training and Support 689
2327:
July 10 - 27 Autism Spectrum Disorder Summer
Program
Days: Monday – Thursday Time: 9:00 am - 12:00
pm
3rd Tuesday, 7 - 9 pm: The Autism Family Support
Group, at the ARC of Lane County
July 17 - 21 Multicultural Camp. See
above for more info.
July 24 - 28 Dance and Art Camp. Also
above.
August 15, 6:30 - 8pm ASO leadership meeting,
Bridgeway House 541-521-7208
August 25-27 KindTree Autism Camp / Retreat.
Details here.
4th Tuesdays Autism Medical Information Support
Group
Oregon Health & Science University - Doernbecher
Children's Hospital - 11th floor Auditorium 503-284-0350
At Bridgeway House: 1st and 3rd Tuesday
nights - Parent support group.
1st Saturdays, 11:30 am: Exploring Aspergers
Syndrome with Nan Lester
September 10, AM. Autism Speaks fundraising
Walk. Help raise funds for autism research.
Contact Teri Baker, Teribaker77436@yahoo.com
|
MARCH,
2006
Community
R Us / Mary-Minn's Stim Page
/ Mental Health and Chemical Dependancy Parity
Computers / Autism From
the Soul / Autism Artism 2006
Art Show in Eugene
Mom Needs Help /Autism
Forum May 20 / Community Calendar
VISIT eSCRIP
and Help Us OUT!! / Or print the sign up form HERE
| 'Community
R Us'
The Autism Community really came through for KindTree this
winter. We received significant donations from Elizabeth
King, George Mueller, Doris Germain, Cheryl Horne, the Wentworth
Foundation, GreyWolf Projects and Mary Ann Hanson. Thank
you all!
Our Computer Exchange Program is benefiting from the technical
expertise of John Wicks (Alpha Omega Computers) and Tim
Savage, both of them working on a group of machines donated
by Lane County. We’ve whittled our waiting list down
to only 6 months and the machines are getting better. Ten
systems were placed in 2005. Keep up the good work!
Our Autism Rocks Traveling Art Show continues to grow, providing
over $1500 in artist payments for last year, including over
$700 in sales of our Holiday Cards. Thanks to all of you
who enjoyed them, and to the talented artists who create
them.
The Art Show also provided grants to 3 artists totaling
$600 as part of our “From the Studio to the Gallery”
program, which cul-minates in the “Autism Artism 2006”
exhibition at DIVA during April, Autism Awareness Month.
16 artists competed with over 100 works for this show, and
our wonderful volunteer jury had a hard time selecting only
25 pictures. The Gala Opening will be a fund-raiser, with
raffle tickets for great gifts, a chance to paint your very
own “autism rock”, and plenty of beautiful art
for sale. Admission is free, so please come. More
here... Special thanks to Karen Howe of LaFollette Gallery
for her indispensable help.
Please note our fifth Autism Forum, coming on May 20. Professionals
from our community will be there to help. This is another
free event, but worth way more. Don’t miss it.
|
|
Kim Miller - Violinist
Poster image for "Autism Artism 2006"
As we began preparations for our the summer,
I came across Dave Kleger, a very active member of the Willamette
Cascade Model Railroad Club. His group is planning a big
show April 8-9 at the Lane County Fairgrounds (only $9 per
family) - and I’m thinking they just might join us
at our Retreat this summer, too. Now, that would be fun!
We’re also working with the Boy Scouts to coordinate
more athletic activities for all the young boys we’ve
hosted there the last few years. I hope that works out,
too. You can make a Re-treat reservation today with the
form below.
Our Autism Community benefits from the efforts of so many
people. Even the Community Village of the Oregon Country
Fair helps us out - we will be selling T-shirts at the Village
Benefit Concert. Joules Graves, Samba Ja, Prezident Brown
and more will rock the McDonald Theatre this April Fool’s
Day. See you there! Do we have too much fun or what?
Tim Mueller |
Just a brief announcement - KindTree's Tim Mueller has retired
from the US Postal Service after 32 years as a Letter Carrier.
Yeeha!
Mary-Minn's
Stim Page
(Here are personal stories
about autism. If you would like to see your musings on this
page, please email Mary-Minn at sirag@mindspring.com.)
On the Illusion
of Leadership
Before I “came out” with
my autism by joining the autism community in late summer,
2000, I wanted nothing more than to be given a chance to
be a Leader. I wanted to spearhead everything from activities
to movements, though I had no specific mission at that point.
All I needed was the authority to lead–or so I thought.
After all, I argued with no one in particular, I was good
at giving feed-back without being judgmental or critical.
The school of hard knocks had taught me not to be a micro-manager.
I had chutzpah. I was fearless about taking responsibility
for my mistakes and learning from them. What more did a
good leader need?
True, I had freakouts, but only when things got out of control.
Granted, I have always been burdened by a stratospheric
standard of “control.” Nonetheless, all I needed
to do was to front-load complex tasks so as not to set my
“team” up to fail by piling on too much at the
last moment. It was a matter of logistics. |
|
"My
frequent brushes with failure in group activities had been
due almost invariably to others’ unenlightened leadership,
or so I thought."
I had written procedure and training manuals, and designed
elaborate work-flow systems as a paranoid precaution against
the chaos and error rate that led to so much blame and dissension
within those harried ranks I was inhabiting.
In the meantime, I had avoided positions of genuine leadership.
Resisting a painfully intense reproductive urge, I had chosen
to forgo starting a family, for fear of finding myself unable
to provide for them financially or to survive the poverty
that my unremark-able wage-earning ability might impose
on my hapless offspring. I had felt righteously responsible
in my decision rather than fearful, as I truly was.
I had turned down one or two opportunities for minor promotions
on the job–out of modesty, I told myself. I had avoided
com-mittees for supposedly esthetic reasons. The word “committee”
was not euphonious to me.
My frequent brushes with failure in group activities had
been due almost invariably to others’ unenlightened
leadership, or so I thought. Back then, I could have written
books on leadership, because I felt omniscient about what
bad leadership looked like from my enlight
| | |